HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297506Generated: October 30, 2026
Ammonium Chloride → 3-(3,5-Dichloro-pyridin-4-ylmethylene)-6-methoxy-1-thiazol-2-yl-1,3-dihydro-isobenzofuran-1-ol
https://huagongshe.com/reaction/2297506
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | HCID 54395392 | HCID 54395392 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3,5-Dichloro-pyridin-4-ylmethylene)-6-methoxy-1-thiazol-2-yl-1,3-dihydro-isobenzofuran-1-ol | HCID 53636271 | 38% |
Reaction Steps
A milky solution of 2-bromothiazole (5.6 g, 34.2 mmoles) in dry ethyl ether (17 ml) was added dropwise to a solution of n-butyl lithium (14.4 ml, 36 mmoles) in dry ethyl ether (50 ml), under N2 at −80° C. The reaction mixture was stirred at −80° C. for 15 minutes, then a solution of 3-(3,5-dichloro-pyridin-4-ylmethylene)-6-methoxy-3H-isobenzofuran-1-one (10 g, 31 mmoles), prepared as described in example 37, in dry THF (60 ml) was slowly added. After 45 minutes at −78° C., the resultant solution was treated with saturated NH4Cl, with water and brought to room temperature. The aqueous phase was separated and extracted with ethyl acetate, decoloured with charcoal, filtered over celite and concentrated under vacuum. The resultant foam was flash cromatographed (eluent petrolatum:ethyl acetate 6:4) obtaining 4.64 g of the title compound (yield: 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06492360B1 |
|---|
| Source dataset | uspto-grants-2002_12 |
|---|
| ORD ID | ord-7067c72834d84f14bf33c5bdef952764 |
|---|
| Source note | uspto-grants-2002_12 |
|---|